meddevicedb.com FDA Device Reference

ANTISERUM TO HUMAN, ALPHA-2-MACROGLOBULI

K790712 Class II Traditional
Decision Date
1979-08-16
Sponsor / Applicant
Kent Laboratories, Inc.

Technical Specification

510(k) Submission ID K790712
Product Code DDB
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5210
Decision Date 1979-08-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANTISERUM TO HUMAN, ALPHA-2-MACROGLOBULI received FDA 510(k) clearance under submission number K790712, sponsored by Kent Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1979-08-16.

Classification & Regulation

This clearance is catalogued under FDA product code DDB and 21 CFR 866.5210, within the Immunology review panel as a Class II device.